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Safety and efficacy of rt-PA treatment for acute stroke in pseudoxanthoma elasticum: the first report

Journal of thrombosis and thrombolysis, 2021, Vol.51 (1), p.176-179

2021

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Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous Malformations

Metabolic brain disease, 2021-10, Vol.36 (7), p.1871-1878

2021

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Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG

BMC neurology, 2020-08, Vol.20 (1), p.1-316, Article 316

2020

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Patient-reported outcome measures in patients with familial cerebral cavernous malformations: results from the Treat_CCM trial

Frontiers in neurology, 2024-02, Vol.15, p.1338941-1338941

2024

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Paroxysmal Nocturnal Hemoglobinuria (Pnh): Brain Mri Ischemic Lesions In Neurologically Asymtomatic Patients

Scientific reports, 2018-01, Vol.8 (1), p.476-476, Article 476

2018

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Genetic Architecture of White Matter Hyperintensities Differs in Hypertensive and Nonhypertensive Ischemic Stroke

Stroke (1970), 2015-02, Vol.46 (2), p.348-353

2015

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A Suspected Case of Cerebral Fat Embolism Triggering a Drug-resistant Status Epilepticus in a HbS/β + -Thalassaemia Patient

Mediterranean journal of hematology and infectious diseases, 2022-03, Vol.14 (1), p.e2022019-e2022019

2022

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Progressive Encephalomyelitis with Rigidity and Myoclonus Associated With Anti-GlyR Antibodies and Hodgkin's Lymphoma: A Case Report

Frontiers in neurology, 2017-08, Vol.8, p.401

2017

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POLG1 mutations and stroke like episodes: a distinct clinical entity rather than an atypical MELAS syndrome

BMC neurology, 2013-01, Vol.13 (1), p.8-8, Article 8

2013

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Molecular basis of young ischemic stroke

Current medicinal chemistry, 2013-10, Vol.20 (31), p.3818-3839

2013

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Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there?

Internal and emergency medicine, 2021-08, Vol.16 (5), p.1247-1252

2021

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Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation

Neurobiology of aging, 2009-05, Vol.30 (5), p.752-758

2009

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Psychiatric Symptoms in Patients with Stroke: A Six-Month Follow-Up Study

Journal of stroke and cerebrovascular diseases, 2016-08, Vol.25 (8), p.2087-2088

2016

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COL4A1 mutations as a monogenic cause of cerebral small vessel disease: a systematic review

Stroke (1970), 2010-08, Vol.41 (8), p.e513-e518

2010

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Optic Neuritis as Isolated Manifestation of Leptomeningeal Carcinomatosis : A Case Report and Systematic Review of Ocular Manifestations of Neoplastic Meningitis

Neurology research international, 2013-01, Vol.2013 (2013), p.1-9

2013

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Antiplatelets vs anticoagulation for dissection: CADISS nonrandomized arm and meta-analysis

Neurology, 2012-08, Vol.79 (7), p.686-689

2012

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Clinical studies in stem cells transplantation for stroke: a review

Current vascular pharmacology, 2010-01, Vol.8 (1), p.29-34

2010

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Intravenous thrombolysis plus endovascular thrombectomy versus thrombolysis alone in large vessel occlusion mild stroke: a propensity score matched analysis

European journal of neurology, 2023-05, Vol.30 (5), p.1312

2023

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Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection

Nature genetics, 2015-01, Vol.47 (1), p.78-83

2015

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Brain Atrophy and Cerebral Small Vessel Disease A Prospective Follow-Up Study

Stroke (1970), 2011, Vol.42 (1), p.133-138

2011

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Intravenous thrombolysis + endovascular thrombectomy versus thrombolysis alone in large vessel occlusion mild stroke: a propensity score matched analysis

European journal of neurology, 2023-05, Vol.30 (5), p.1312-1319

2023

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The role of clinical and neuroimaging features in the diagnosis of CADASIL

Journal of neurology, 2018-12, Vol.265 (12), p.2934-2943

2018

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Magnetic susceptibility as a 1-year predictor of outcome in familial cerebral cavernous malformations: a pilot study

European radiology, 2023-06, Vol.33 (6), p.4158-4166

2023

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Improving clinical interpretation of five KRIT1 and PDCD10 intronic variants

Clinical genetics, 2021-06, Vol.99 (6), p.829-835

2021

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Safety and efficacy of rt-PA treatment for acute stroke in pseudoxanthoma elasticum: the first report

Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous Malformations

Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG

Patient-reported outcome measures in patients with familial cerebral cavernous malformations: results from the Treat_CCM trial

Paroxysmal Nocturnal Hemoglobinuria (Pnh): Brain Mri Ischemic Lesions In Neurologically Asymtomatic Patients

Genetic Architecture of White Matter Hyperintensities Differs in Hypertensive and Nonhypertensive Ischemic Stroke

A Suspected Case of Cerebral Fat Embolism Triggering a Drug-resistant Status Epilepticus in a HbS/β + -Thalassaemia Patient

Progressive Encephalomyelitis with Rigidity and Myoclonus Associated With Anti-GlyR Antibodies and Hodgkin's Lymphoma: A Case Report

Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA project

POLG1 mutations and stroke like episodes: a distinct clinical entity rather than an atypical MELAS syndrome

Molecular basis of young ischemic stroke

Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there?

Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation

Psychiatric Symptoms in Patients with Stroke: A Six-Month Follow-Up Study

COL4A1 mutations as a monogenic cause of cerebral small vessel disease: a systematic review

Optic Neuritis as Isolated Manifestation of Leptomeningeal Carcinomatosis : A Case Report and Systematic Review of Ocular Manifestations of Neoplastic Meningitis

Antiplatelets vs anticoagulation for dissection: CADISS nonrandomized arm and meta-analysis

Clinical studies in stem cells transplantation for stroke: a review

Intravenous thrombolysis plus endovascular thrombectomy versus thrombolysis alone in large vessel occlusion mild stroke: a propensity score matched analysis

Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection

Brain Atrophy and Cerebral Small Vessel Disease A Prospective Follow-Up Study

Intravenous thrombolysis + endovascular thrombectomy versus thrombolysis alone in large vessel occlusion mild stroke: a propensity score matched analysis

The role of clinical and neuroimaging features in the diagnosis of CADASIL

Magnetic susceptibility as a 1-year predictor of outcome in familial cerebral cavernous malformations: a pilot study

Improving clinical interpretation of five KRIT1 and PDCD10 intronic variants

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